After years of uncertainty following Brexit and extensive discussions across the medical device industry, the wait is finally over. The UK Gove...
Exclusive Webinar with Mandala I Expanding into South America?
Explore regulatory requirements, market entry strategies and product registration opportunities across Latin America. Expanding into South America off...
Insights from a Software-Focused Notified Body
In this expert webinar, MDSS explores the regulatory perspective on software and software-focused medical devices with insights from a Notified Body. ...
EUDAMED: The 60-Day Challenge
With the mandatory EUDAMED registration deadline approaching, manufacturers need to ensure that their device data and registration activities are read...
